Monday, April 30, 2012

Muscular Dystrophy Funraiser At Licks in Bronte

The Halton Region Walk for Muscular Dystrophy Planning Committee wishes to thank Jon Hall @LicksBronte Owner and staff of Lick's Bronte for hosting a $1 Burger Event Saturday, April 28, 2012. They rolled out the red carpet for us which allowed us to raise awareness for Muscular Dystrophy Canada and our 3 annual fund raising walk coming up Sunday, May 6, 2012 at Coronation Park, Oakville. Please check back soon for amount raised!  Thank you for your Support and see you at the walk!

Thursday, April 26, 2012

Muscles Needed For Walk For Muscular Dystrophy

 Apr 25, 2012 Oakville Beaver

On Sunday, May 6 Halton residents will be moving their muscles to make an impact in the fight against muscular dystrophy.

The community will be joining together for the annual Halton Region Walk for Muscular Dystrophy to support more than 50,000 children, teens and adults who are affected by neuromuscular disorders in Canada.

Leading the Halton Region event will be this year’s Walk Ambassador Shanna Bernacki, of Burlington, who knows firsthand how important this community event is to families affected by muscular dystrophy. 
“It’s nice to meet other people taking part in the walk that are going through the same as me and being able to share experiences. It gives me the sense… that I’m not alone,” said Bernacki, who was diagnosed with Friedreich’s Ataxia (a rare disease affecting the heart and muscles) at the age of nine. Muscular dystrophy refers to a group of progressive muscular disorders that weaken the muscles that control body movement.

These disorders can have devastating affects, resulting in the loss of most abilities we take for granted. Over time, many people with neuromuscular disorders are unable to walk, speak or even breathe. For some, the disorder is fatal.

The Walk for Muscular Dystrophy is “an opportunity for the community to come together and support those affected by neuromuscular disorders at the local level,” said Stacey Lintern, Muscular Dystrophy Canada Ontario executive director.

The walk is a fun-filled, fully-accessible event the entire family can enjoy, regardless of fitness level.The event will include activities for kids, food and refreshments, a prize raffle and silent auction, and even a visit from local firefighters.

Proceeds from the event support various programs including funding equipment and support services for individuals and families faced with financial hardships, information and advocacy initiatives that highlight the needs of those living with neuromuscular disorders, and fund research to one day find a cure.All of Muscular Dystrophy Canada’s programs are made possible by donations. The organization receives less than one per cent in government funding.

Festivities will be taking place on Sunday, May 6 at Coronation Park.
Participant registration begins at 10 a.m. and the walk, wheel and roll begins at 11 a.m. To take part in the Halton Region Walk for Muscular Dystrophy or for more information, visit www.muscle.ca/walk.



Thursday, April 12, 2012

A Lick's Burgar Day


The Halton Walk for Muscular Dystrophy is setting up "A Lick's Burgar Day"  on Saturday, April 28 from 11:00am to 5:00pm at Bronte Licks 2420 Lakeshore Rd W, Oakville, ON and $1 from every beef or nature burger will go to Muscular Dystrophy!

We will be spreading the word about MD and raising awareness for the 3rd Annual Walk for MD, May 6th at CoronationPark, Oakville.  We will be located right at the front of the restaurant.  So please drop by, enjoy some family time and remember $1 goes towards MD Canada.

3rd Annual Halton Region Walk for Muscular Dystrophy
Sunday, May 6, 2012 Corontation Park, Oakville

ONLINE REGISTRATION http://muscle.akaraisin.com/haltonregionWMD2012/186d4621b1524f8e99731ff8c2929cdd?abcId=2047156&TV=1

Let us know you will be attending here on Facebook as well as our EVENTBRITE PAGE http://licksraisingawareness.eventbrite.ca/

 

Tuesday, March 13, 2012

Halton Walk for Muscular Dystrophy

Last year the Walk for Muscular Dystrophy raised over $1,080,000 in 55 locations across Canada. In 2012, we will celebrate the 5th annual Walk for Muscular Dystrophy as our national signature fundraising event in support of Canadians affected by neuromuscular disorders.

Help make a difference by registering for the Halton Region Walk for Muscular Dystrophy at http://www.muscle.ca/walk and help raise funds to support those living with a neuromuscular disorder in your community. 

3rd Annual Halton Region Walk for Muscular Dystrophy will be May 6th at Coronation Park Oakville!!!  32 more days before the Walk begins.  Get your walking shoes on! Look forward in seening you there!

We are excited that Rita Carrey is joining us as as the Honorary Chair for the 2012 Halton Region Walk for Muscular Dystrophy from Giant FM Classic Rock






PSA from Global Toronto featuring Anthony Farnell...have you seen this on Global TV yet?

For more information or if you would like to get involved in the Planning Committee, please contact us at: walkformusculardystrophy.on@muscle.ca

Together, we can Make Muscles Move!

 

Make your own slide show at Animoto.

Monday, March 5, 2012

Pickering Students Raise $19K in Memory of Mitchell Wilson



Mitchell Wilson, who suffered from muscular dystrophy, took his own life last September after he was bullied by students at his Pickering school. Students throughout Pickering raised more than $19,000 in his memory for other children who suffer from muscular dystrophy.
Pickering students amazed even themselves when they handed over a cheque for more than $19,000 to help local kids suffering from muscular dystrophy. 

Their charity, I Am Who I Am, was created only four months ago by a group of students at Pine Ridge Secondary School in memory of Mitchell Wilson, an 11-year-old boy who suffered from the disease and tragically took his own life last fall after he was bullied. 

The project has since been adopted by all 19 schools in the Pickering public board, and sells t-shirts and wristbands to promote acceptance in schools and raise money for cancer research and muscular dystrophy. 

The group’s original goal was to raise $10,000 to buy one wheelchair. But after meeting with Muscular Dystrophy organizations — and surpassing that goal in just one month — the group realized they could make an even bigger difference.

Students handed over a cheque on Friday for almost twice that — $19,341.48 — to Muscular Dystrophy Canada, with funds going to seven local families with children suffering from the disease.

“Everybody was happy to see that within four months we’ve changed people’s perception of one another,” said student leader and Pine Ridge Grade-12-student Cody Morrison. “And we’ve raised a lot of money along the way that’s going to help a lot of people.”

Their green “I Am Who I Am” t-shirts have been donned by the likes of Defence Minister Peter MacKay, Premier Dalton McGuinty — and one even made it to the top of Mount Kilimanjaro. Morrison, 18, said their charity got a nod at the provincial Legislature by MPP Joe Dickson, and at the House of Commons by MP Chris Alexander. 

“Once you accomplish something like that the feeling is pretty indescribable,” Morrison said. Pine Ridge Principal Debbie Johnson said everyone at the ceremony Friday was touched and emotions were high at the school.

Mitchell’s father, Craig Wilson, was there to present a plaque to the association in memory of Mitchell on behalf of the Pickering schools.

Mitchell took his own life in September after he found out he would have to testify in court against a fellow student who’d allegedly assaulted and robbed him while he was out on his daily walk to maintain his mobility skills. 

A verdict in the case is expected on Monday.
The Star Published On Sun Mar 04 2012
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Please show your support at the Halton Region Walk for Muscular Dystrophy and meet your local Ambassadors! Raise awareness of the Walk for Muscular Dystrophy in their community on May 6th, 2012 at Coronation Park Oakville or contact Stephanie Fenyes, walkformusculardystrophy.on@muscle.ca

Tuesday, January 10, 2012

2012 Halton Region Walk for Muscular Dystrophy


About the Walk for Muscular Dystrophy

The Walk for Muscular Dystrophy is Muscular Dystrophy Canada’s national signatur­e event held in over 55 local communities across the country. In 2012, 15 Walk for Muscular Dystrophy events will be taking place in Ontario.

The Walk for Muscular Dystrophy is a family fun event that helps raise funds to support those living with a neuromuscular disorder in your community. Funds raised will support Muscular Dystrophy Canada’s mobility equipment program, education, research and advocacy initiatives and fund ground breaking research to one day find a cure.

Did you know?

More than 50,000 Canadians are affected by neuromuscular disorders.

There are more than 160 neuromuscular disorders under the umbrella of muscular dystrophy, which refers to a group of genetic muscle disorders that are characterized by progressive weakness and wasting of the voluntary muscles that control body movement.

Children, teens and adults who live with these disorders gradually lose the ability to do most things we take for granted, like walking or getting up from a chair.

Muscular dystrophy can also lead to shortened life expectancy. Currently there is no cure.

There are more than 75 people affected by a neuromuscular disorder living in Halton Region.


2012 Halton Region Walk for Muscular Dystrophy

What: 1k or 5k walk, wheel, roll or run!
When: Sunday, May 6th, 2012
Where: Coronation Park in Oakville, Ontario
Time: Registration opens at 10 a.m., walk begins at 11 a.m.
For more information on how to get involved, please visit www.muscle.ca/walk
Halton Region Walk for Muscular Dystropy - Coronation Park Oakville Ontario
 

Saturday, November 5, 2011

Amazing Race to support boy and those with DMD

While some donors are sometimes skeptical if their charitable dollars are really making an impact, a young Oakville boy with Duchenne Muscular Dystrophy (DMD) is living proof that a local fundraiser is indeed making a difference, close to home.

Dianne Cornish, Flamborough Review- Oct 27, 2011 - http://www.insidehalton.com/


Amazing Race to support boy and those with DMD. RAISING HELP: Pictured is Eric Morden (centre) who is living with Duchenne muscular dystrophy, flanked by his aunt and uncle Ted Lindsay and Heather Johnston. Submitted photo
While some donors are sometimes skeptical if their charitable dollars are really making an impact, a young Oakville boy with Duchenne muscular dystrophy (DMD) is living proof that a local fundraiser is indeed making a difference, close to home.

Eleven-year-old Eric Morden is past the age where most afflicted with the disease are unable to walk and yet, he continues to walk with the help of medications. This year, he was chosen to be part of a major double blind study for boys with DMD.

“The fact that this test is available in London (Ontario) can be directly linked to Jesse’s Journey and even some of the research dollars raised by Eric’s Amazing Race,” said Burlington resident Ted Lindsay, Eric’s uncle and advertising manager at a Metroland newspaper. “To quote Jesse Davidson, ‘people should work together to make research happen because when people work together miracles happen,’” he added.
Lindsay and his wife, Heather Johnston, founded Eric’s Amazing Race, a local car rally and silent auction, after learning of their nephew’s diagnosis with the disorder in November 2002. Rather than accept the news passively, they decided to face it head-on by organizing a fundraiser in support of research into the disorder characterized by muscle degeneration, loss of ambulation and eventually death.

The rally that runs along north Flamborough and Burlington roads when the autumn colours are at their prime seemed like the perfect event to support the cause as research into a cure is indeed a race against time.
The ninth annual Eric’s Race will be held Saturday, Nov. 5, starting about 1 p.m. at Bruce T. Lindley School, 2510 Cavendish Dr. in north Burlington and ending at the Waterdown Legion, where the auction will be held from 3 until 7 p.m.

Registration of race participants will start at the Burlington school at noon. The cost is $10 per person.
Last year’s turnout for the rally was a record, with 40 cars registering, representing a total of 120 participants. Most years, the rally attracts about 30 cars or 100 participants.

Over the past eight years, the event has raised more than $120,000, with all funds going to Jesse’s Journey, a charitable organization that raises funds for research into DMD and gene and stem cell therapies.
The foundation is named after Jesse Davidson, a London man who lost his life to DMD at age 29, just the day before the 2009 race. For more information, visit online at www.jessesjourney.com.
“It’s a very family-friendly event,” Lindsay said of the rally and auction while lauding the support that he and his wife get every year from family and friends.

The auction, which drew close to 500 guests last year, features about 200 items donated by local businesses and individuals, including everything from tickets to Hamilton Bulldog games or the Ontario Science Centre to gift certificates and sports memorabilia. This year, several pieces of equipment autographed by hockey great Mario Lemieux will be up for auction.

Also new this year will be live entertainment by Semitone, a Burlington-based band composed of two acoustic guitar players who will entertain the crowd with classic rock.Lindsay said those who come out to support Eric’s Amazing Race can be assured that their support is having an impact.

“Literally, every dollar makes a difference, ” he said, adding that he’s convinced that research into the disorder has enabled his nephew to remain agile and mobile rather than bound to a wheelchair.
“He’s living it and he’s beating it, and that’s pretty cool,” he said of Eric’s battle with DMD.
According to Rick Moss, managing director of Jesse’s Journey, Eric and other boys are involved in a 52-week double blind study headed up by Dr. Craig Campbell at the Children’s Hospital in London. Eric gets shots there every week to help with muscle regeneration.

Moss said the study will prove helpful for those suffering from other neuromuscular diseases, such as ALS (Amyotrophic Lateral Sclerosis) and MS (Multiple Sclerosis). He added that funds raised at Eric’s Amazing Race have been a great support for research and trials that are helping improve the lives of close to 2,000 boys afflicted with DMD across Canada.

For more information about the fundraiser or to make a donation either to Jesse’s Journey or the auction, please contact Lindsay at 905-331-6874